一名精神分裂症患者急性一氧化碳中毒后迟发性神经精神后遗症的鉴别诊断和预后:病例报告。

PCN reports : psychiatry and clinical neurosciences Pub Date : 2024-06-22 eCollection Date: 2024-06-01 DOI:10.1002/pcn5.218
Yuto Satake, Yoshimasa Mamiya, Shizuka Kano, Katsuhiko Akizuki, Mamoru Hashimoto, Manabu Ikeda
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引用次数: 0

摘要

背景:迟发性神经精神后遗症(DNS)是急性一氧化碳(CO)中毒数天至数周后出现的一种综合征。DNS 表现为各种神经精神症状,如精神衰退和帕金森病:我们的病例是一名患有精神分裂症的 37 岁男性。病例介绍:我们的病例是一名患有精神分裂症的 37 岁男性,他因 CO 中毒而试图自杀,被送到我们的急诊科(第 0 天)。他接受了为期 3 天的常压氧通气治疗,在意识清楚的情况下被转入精神科病房。我们重新开始使用抗精神病药物,他逐渐出现了运动障碍和僵直。此外,在第 32 天左右,他出现了行为紊乱、精神衰退、大小便失禁和步态障碍。第 35 天,脑磁共振成像(MRI)显示略有异常。虽然我们根据临床表现和核磁共振成像结果怀疑是 DNS,但也考虑了紧张症和抗精神病药物的副作用。最后,在第 38 天,脑电图(EEG)出现明显异常,包括弥漫性慢波,我们诊断他患有 DNS,并对他进行了高压氧治疗。他的病情明显好转,脑电图上的弥漫性慢波在第 83 天消失。我们还对他的临床表现和脑部核磁共振成像进行了跟踪,直至 33 个月。在整个随访期间,他的认知、运动和精神症状保持稳定。然而,在整个病程中,他的脑部核磁共振成像显示双侧额叶进行性萎缩,白质病变不断增加:结论:脑电图和脑核磁共振成像可能是对患有药物治疗和严重精神疾病的复杂病症患者进行 DNS 鉴别诊断的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential diagnosis and prognosis of delayed neuropsychiatric sequelae after acute carbon monoxide poisoning in a patient with schizophrenia: A case report.

Background: Delayed neuropsychiatric sequelae (DNS) is a syndrome that appears days to weeks after acute carbon monoxide (CO) poisoning. DNS shows various neuropsychiatric symptoms, such as mental deterioration and parkinsonism.

Case presentation: Our case was a 37-year-old male with schizophrenia. He attempted suicide by CO poisoning and was brought to our emergency department (Day 0). He was ventilated with normobaric oxygen therapy for 3 days and moved to the psychiatric ward with clear consciousness. We restarted antipsychotics, and he gradually presented akinesia and rigidity. Additionally, around Day 32, he showed disorganized behaviors, mental deterioration, incontinence, and gait disturbance. Brain magnetic resonance imaging (MRI) showed slightly abnormal findings on Day 35. Although we suspected DNS on the clinical course and the MRI findings, catatonia and side-effects of antipsychotics were also considered. Finally, electroencephalography (EEG) on Day 38 with apparent abnormalities, including diffuse slow waves, resulted in our diagnosis of DNS, and he underwent hyperbaric oxygen therapy. His condition was dramatically improved, and his diffuse slow waves on EEG disappeared on Day 83. We also followed his clinical presentations and brain MRI until 33 months. Throughout the whole follow-up, his cognition, movement, and psychiatric symptoms remained stable. However, his brain MRI showed progressive atrophy in bilateral frontal lobes and increasing white matter lesions throughout the whole course.

Conclusion: EEG, as well as brain MRI, may be crucial in the differential diagnosis of DNS in patients with complex conditions involving medications and severe mental illnesses.

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